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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16746생성일: 2026년 10월 24일

Chloride → HCID 178497986, 화합물

https://huagongshe.com/ko/reaction/16746

반응식

참여 물질

역할이름HCID투입량
반응물ChlorideHCID 312—
반응물DichloromethaneHCID 6344—
반응물5-(Methoxycarbonyl)pyridine-2-carboxylic acidHCID 314992—
반응물Tert-butyl 5-amino-3-[2-(3-methoxyphenyl)ethyl]pyrazole-1-carboxylateHCID 57440385—
촉매DimethylformamideHCID 6228—
용매Formic AcidHCID 284—
용매PyridineHCID 1049—
용매AcetonitrileHCID 6342—
생성물HCID 178497986HCID 178497986—

반응 단계

5-Methoxycarbonylpyridine-2-carboxylic acid (0.285 g, 1.58 mmol) was added to DCM (40 ml), to this was added oxayl chloride (0.165 ml, 1.90 mmol) and a few drops of anhydrous DMF. The reaction mixture was stirred for 30 mins before the addition of tert-butyl 5-amino-3-[2-(3-methoxyphenyl)ethyl]pyrazole-1-carboxylate (0.50 g, 1.58 mmol) and pyridine (2.0 ml). The reaction was stirred overnight. The reaction was evaporated to dryness to give yield to a gum. To this gum was added formic acid. The reaction mixture was stirred for 1 h before being evaporated to dryness. The resulting gum was quenched with saturated potassium carbonate (30 ml), extracted with DCM (3×50 ml), dried (MgSO4) and the solvent removed in vacuo to yield a viscous gum. Trituration with acetonitrile gave the desired product as a slightly yellow solid (24 mg, 4%); 1H NMR (400.132 MHz, DMSO) δ 2.92 (s, 4H), 3.74 (s, 3H), 3.95 (s, 3H), 6.50 (s, 1H), 6.76 (d, 1H), 6.83-6.82 (m, 2H), 7.20 (t, 1H), 8.26 (d, 1H), 8.53 (d, 1H), 9.17 (s, 1H), 10.38 (s, 1H), 12.31 (s, 1H); MH+381.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737149B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-63b3fc2d6288449b873b2484e424d16f
출처 메모uspto-grants-2010_06